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3,4-Dichloro-6-(Trifluoromethyl)Toluene

    • Product Name 3,4-Dichloro-6-(Trifluoromethyl)Toluene
    • Alias 3,4-Dichloro-6-(trifluoromethyl)benzyl
    • Einecs 245-986-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    363479

    Productname 3,4-Dichloro-6-(Trifluoromethyl)Toluene
    Casnumber 393-98-0
    Molecularformula C8H5Cl2F3
    Molecularweight 229.03 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 176-178 °C
    Meltingpoint -1 °C
    Density 1.433 g/cm3
    Refractiveindex 1.516
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in organic solvents
    Smiles CC1=C(C=C(C(=C1)Cl)Cl)C(F)(F)F

    As an accredited 3,4-Dichloro-6-(Trifluoromethyl)Toluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, white label with hazard symbols and barcode, 100g net, "3,4-Dichloro-6-(Trifluoromethyl)Toluene" printed clearly.
    Shipping 3,4-Dichloro-6-(Trifluoromethyl)Toluene should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Comply with all relevant hazardous material regulations during transit, including proper labeling and documentation. Use secondary containment and cushioning to prevent leaks or spills. Ship at ambient temperature unless otherwise specified by the safety data sheet (SDS).
    Storage Store **3,4-Dichloro-6-(Trifluoromethyl)Toluene** in a tightly sealed container, in a cool, dry, well-ventilated area away from heat sources, ignition sources, and incompatible materials such as strong oxidizers. Protect from direct sunlight and moisture. Label containers clearly and keep away from food and drink. Use appropriate secondary containment to prevent environmental release in case of spills or leaks.
    Application of 3,4-Dichloro-6-(Trifluoromethyl)Toluene

    Applications of 3,4-Dichloro-6-(Trifluoromethyl)Toluene in Industrial Manufacturing

    We supply 3,4-Dichloro-6-(Trifluoromethyl)Toluene for advanced chemical synthesis routes across key industrial sectors. As a direct manufacturer, we focus on consistent quality, batch traceability, and proven utility in demanding downstream production environments. Below, we detail main application segments based on current industry practice.

    1. Agrochemical Active Ingredient Synthesis

    This raw material serves as a primary intermediate for the synthesis of selective herbicide and insecticide actives, especially within chloro- and fluorinated compound families. Process engineers incorporate it during multi-stage acylation, halogenation, and coupling reactions to build complex molecules targeting specific pest and weed species. Detailed impurity profiles and specification controls allow manufacturers to meet agrochemical market requirements for both technical-grade and formulation batches.

    Industry compliance standards

    • FAO and WHO pesticide specification guidelines
    • ISO 9001:2015 quality management system
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA registration standards for pesticide intermediates

    Typical usage ratio

    • 10–25% as a core building block, adjusted according to molecular design and target compound yield

    Downstream process integration

    • Introduced after diazotization or Friedel–Crafts alkylation steps
    • Acts as the halogen donor or aromatic partner in synthesis reactions
    • Employed under controlled temperature and sealed reactor environments

    Final product types

    • Herbicidal active technical (e.g., chloro-fluoro aromatics)
    • Pyridine or pyrimidine insecticide precursors
    • Pre-final intermediates shipped for formulation into wettable powders or ECs

    2. Pharmaceutical Intermediate Manufacturing

    Our material is in demand as a precursor for advanced pharmaceutical intermediates, primarily for synthesizing APIs containing multi-halogenated aromatic rings. It enters GMP-regulated synthesis steps producing small-molecule drugs, typically those targeting CNS or oncology indications. Due to strict regulatory control, trace-level impurity documentation and certificate of analysis are provided with every batch.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API manufacturing
    • USP/EP/JP monograph reference for raw materials
    • 21 CFR Part 211 for pharmaceutical quality systems
    • REACH registered for use in pharma synthesis

    Typical usage ratio

    • 5–15% in stepwise halogenated aromatic coupling reactions, modified by target molecule backbone

    Downstream process integration

    • Charged post-coupling with nucleophilic agents during stepwise synthesis
    • Integrated with in situ purification and continuous flow reactors
    • Subject to full-inventory reconciliation due to GMP traceability

    Final product types

    • API intermediates for antipsychotics and anticancer drugs
    • Key ring systems in custom pharma synthesis
    • Substituted anilines or trifluoromethylated analogues for further finishing

    3. Advanced Dye and Pigment Synthesis

    Specialty colorant manufacturers use this raw material as an aromatic starting material for synthesizing high-performance dyes and pigments. Its trifluoromethyl group enhances color fastness and thermal stability. QC teams monitor exact chloride and fluorine content, as it directly impacts hue, purity, and environmental compliance in end-use textiles and plastics.

    Industry compliance standards

    • EN 71-3 Safety of Toys – migration of certain elements
    • OEKO-TEX® Standard 100 for textile dye safety
    • ISO 9001 and 14001 certified pigment production
    • GB/T 23986-2009 for organic pigment manufacturing

    Typical usage ratio

    • 15–30% in azo or phthalocyanine dye production, fine-tuned by shade intensity and carrier composition

    Downstream process integration

    • Introduced in coupling or condensation stages after halogen balancing
    • Used as a key halogenated aromatic for molecular modification
    • Subjected to heat-treated filtration and crystallization post-synthesis

    Final product types

    • High-stability textile dyes (e.g., for polyester fiber)
    • Thermally stable plastic colorants
    • Special effect pigments with improved lightfastness

    4. Electronic Chemical Processing (Semiconductor Grade)

    In the electronics industry, our material meets the trace purity specifications required for the manufacture of halogenated precursors used in advanced etchants and photoresist systems. Production lines employ it for introducing precise functional groups within semiconductor fabrication. Every batch undergoes high-resolution purity analysis to ensure low metal and ionic contaminant levels, crucial for wafer production.

    Industry compliance standards

    • SEMI C69 specification for wet chemicals used in electronics
    • RoHS Directive 2011/65/EU (lead, mercury, cadmium content)
    • ISO 9001:2015 specialized for electronic chemical supply
    • Customer-specific material acceptance criteria (e.g., maximum 1 ppb metal content)

    Typical usage ratio

    • 2–10% as a functionalized aromatic intermediate for custom etchants and resist agents; adjusted by process purity requirements

    Downstream process integration

    • Dispensed directly into micro-patterned coating or etching steps
    • Filtered through sub-micron purity systems before entering spin-coating or vapor deposition
    • Records maintained for each production lot for traceability

    Final product types

    • Semiconductor photoresists and masks
    • Circuit etchants for printed circuit board fabrication
    • Microelectronic passivation agents

    5. Specialty Polymer Modifier Manufacturing

    Producers of flame-retardant or chemical-resistant polymer compounds leverage this raw material as a halogen-rich modifier during polymer backbone synthesis. Its involvement enhances polymer matrix stability, mechanical attributes, and thermal limits. Polymer scientists integrate it under inert gas protection with precise mixing ratios to develop performance polymers used in wire and cable insulation, automotive interiors, and high-demand construction materials.

    Industry compliance standards

    • UL 94 flammability testing for plastics
    • REACH Annex XVII restricted substances compliance
    • ISO 1043-4 polymer designation reporting
    • EPA TSCA polymer exemption rule documentation

    Typical usage ratio

    • 8–20% depending on the final polymer matrix and desired flame retardance or resistance levels; evaluated through laboratory performance testing

    Downstream process integration

    • Blended during copolymerization as a chain modifier
    • Extruded as a melt additive under nitrogen atmosphere
    • Monitored for residual monomer removal in finishing

    Final product types

    • Flame-retardant electrical cable coatings
    • Resistant automotive interior plastics
    • Chemical-resistant building panels

    6. Veterinary Active Intermediate Production

    Animal health pharmaceutical manufacturers utilize this material as a specialized building block in veterinary drug synthesis, especially for compounds requiring halogenated aromatic moieties. Production steps require strict feedstock validation to meet VICH and OCDE residue standards. Detailed batch records support their application in animal-use formulations.

    Industry compliance standards

    • VICH GL 10 GMP guidelines for veterinary drugs
    • OECD Test Guidelines for residue and impurity determination
    • Directive 2001/82/EC (EU rules for veterinary medicine)
    • ISO 17025-accredited analytical testing for intermediates

    Typical usage ratio

    • 5–18% depending on the final molecule’s structure and residual impurity control

    Downstream process integration

    • Introduced in third- or fourth-step syntheses to construct active core structures
    • Subjected to phase-transfer catalysis or selective reduction following introduction
    • Purified with column chromatography as per VICH controls

    Final product types

    • Antiparasitic veterinary actives
    • Halogenated intermediates for anti-inflammatory veterinary agents
    • Technical-grade compounds for further formulation
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